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HRID 256578Erstellt: 25. Oktober 2026

Benzene, 1-fluoro-2-(trifluoromethyl)- → 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane

https://huagongshe.com/reaction/256578

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-fluoro-2-(trifluoromethyl)-HCID 9807—
Edukt(+-)-3-QuinuclidinolHCID 15381—
EduktSodium hydrideHCID 24758—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octaneHCID 1019933379%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A solution of 1.78 g (14 mmol) of 3-quinuclidinol in 20 ml of dry N,N-dimethylformamide (DMF) was added dropwise under nitrogen to a suspension of 0.6 g (15 mmol) of sodium hydride in 20 ml of dry DMF. The mixture was stirred for 15 min at 70° C., and a solution of 3.8 ml (30 mmol) of 2-fluoro-(trifluoromethyl)benzene in 8 ml of dry DMF was added dropwise. The mixture was stirred for another 1.5 h, after which the solvent was evaporated. The residue was dissolved in ethyl acetate and washed with brine. The ethyl acetate layer was separated, dried over magnesium sulfate and evaporated to dryness. The crude compound was purified by column chromatography on silica using methanol-dichloromethane (2:8) as eluent to give 3.0 g (59% yield) of 3-[2-(trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2 ]octane, which was converted into the oxalate salt by treatment with oxalic acid and recrystallization from methanol. m.p. 174° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05258392
Quelldatensatzuspto-grants-1993_11
ORD IDord-ec0a81e2fdd044d89fb54e6141d93b73
Quellennotizuspto-grants-1993_11